Class 3 Medicines Recall: Sun Pharmaceutical Industries Limited, Fingolimod Sun 0.5mg Hard Capsules, El(25)a/49
Recall Summary Sun Pharmaceutical is recalling a single batch of Fingolimod SUN 0.5mg capsules (batch EL(25)A/49) distributed in the United Kingdom because capsules are breaking when removed from the blister pack. This recall affects only this one batch; other batches of the same medication are not impacted.
- Recalling firm
- Sun Pharmaceutical Industries Limited
- Reason
- Sun Pharma UK Limited is conducting a precautionary recall of a single batch of Fingolimod SUN 0.5 mg hard capsules due to reports of capsule breakage on removing from the blister. No other batches of Fingolimod SUN 0.5mg hard capsules are impacted.
- Classification
- Class II
- Category
- drug recall
- Country
- United Kingdom
- Agency
- UK Medicines and Healthcare products Regulatory Agency
- Recall date
- 2025-11-20
- Status
- Ongoing
- Distribution
- United Kingdom
Official recall notice from UK Medicines and Healthcare products Regulatory Agency
Recall details on Nibble Recalls: https://trynibble.app/recalls/f8846884-54f7-494d-bb07-3124be6a7bfd